Variant report

Variant	nsv829977
Chromosome Location	chr4:79082318-79110300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:353)
CpG islands
(count:794)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:79097596-79098142	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:79086728-79087416	HepG2	liver:	n/a	n/a
3	BHLHE40	chr4:79097626-79097968	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:79100452-79100644	GM12878	blood:	n/a	chr4:79100516-79100525 chr4:79100516-79100525 chr4:79100517-79100526 chr4:79100514-79100527
5	BHLHE40	chr4:79097712-79097922	HepG2	liver:	n/a	n/a
6	BHLHE40	chr4:79097581-79098214	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:79097699-79098020	A549	lung:	n/a	chr4:79097866-79097877
8	CEBPB	chr4:79097633-79098082	A549	lung:	n/a	chr4:79097866-79097877
9	CEBPB	chr4:79097649-79098122	ECC-1	luminal epithelium:	n/a	chr4:79097866-79097877
10	CEBPB	chr4:79097664-79098003	ECC-1	luminal epithelium:	n/a	chr4:79097866-79097877
11	CEBPB	chr4:79097686-79098307	HepG2	liver:	n/a	chr4:79097866-79097877
12	CEBPB	chr4:79086892-79087242	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:79086962-79087265	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:79097624-79097988	HepG2	liver:	n/a	chr4:79097866-79097877
15	CEBPB	chr4:79086929-79087362	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:79086925-79087301	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:79097566-79098221	MCF-7	breast:	n/a	chr4:79097866-79097877
18	CEBPB	chr4:79097438-79098246	Hela-S3	cervix:	n/a	chr4:79097866-79097877
19	CEBPB	chr4:79097616-79098304	HepG2	liver:	n/a	chr4:79097866-79097877
20	CEBPB	chr4:79097728-79097956	HepG2	liver:	n/a	chr4:79097866-79097877
21	CEBPB	chr4:79097563-79098106	A549	lung:	n/a	chr4:79097866-79097877
22	CEBPB	chr4:79097519-79098312	MCF-7	breast:	n/a	chr4:79097866-79097877
23	CEBPD	chr4:79097725-79097907	HepG2	liver:	n/a	n/a
24	CHD2	chr4:79087940-79088004	GM12878	blood:	n/a	n/a
25	CTCF	chr4:79100120-79100270	GM12868	blood:	n/a	n/a
26	CTCF	chr4:79092780-79092930	GM12878	blood:	n/a	n/a
27	CTCF	chr4:79092772-79092894	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr4:79092817-79092825	GM19238	blood:	n/a	n/a
29	CTCF	chr4:79092752-79092915	MCF-7	breast:	n/a	n/a
30	CTCF	chr4:79092760-79092910	HEK293	kidney:	n/a	n/a
31	CTCF	chr4:79092740-79092890	A549	lung:	n/a	n/a
32	CTCF	chr4:79092679-79092917	K562	blood:	n/a	n/a
33	CTCF	chr4:79092660-79092810	BE2_C	brain:	n/a	n/a
34	CTCF	chr4:79092763-79092921	K562	blood:	n/a	n/a
35	CTCF	chr4:79092803-79092883	LNCaP	prostate:	n/a	n/a
36	CTCF	chr4:79092826-79092851	GM19238	blood:	n/a	n/a
37	CTCF	chr4:79092740-79092890	GM06990	blood:	n/a	n/a
38	CTCF	chr4:79092663-79092981	K562	blood:	n/a	n/a
39	CTCF	chr4:79092720-79092922	HepG2	liver:	n/a	n/a
40	CTCF	chr4:79092660-79092810	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:79092793-79092858	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:79092700-79092850	HMF	breast:	n/a	n/a
43	CTCF	chr4:79092770-79092909	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:79092612-79092919	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr4:79092623-79092930	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr4:79092700-79092850	GM12873	blood:	n/a	n/a
47	CTCF	chr4:79092792-79092880	HepG2	liver:	n/a	n/a
48	CTCF	chr4:79092720-79092870	HCT-116	colon:	n/a	n/a
49	CTCF	chr4:79092800-79092909	NHEK	skin:	n/a	n/a
50	CTCF	chr4:79092780-79092930	HRPEpiC	eye:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:79106308-79106358	RPTEC	kidney:	n/a
2	chr4:79106308-79106358	RPTEC	kidney:	n/a
3	chr4:79083545-79083595	IMR90	lung:	fetal
4	chr4:79096535-79096585	MCF10A-Er-Src	breast:	n/a
5	chr4:79102901-79102951	HRE	kidney:	n/a
6	chr4:79103126-79103176	A549	lung:	n/a
7	chr4:79103290-79103340	MCF-7	breast:	n/a
8	chr4:79103290-79103340	A549	lung:	n/a
9	chr4:79103030-79103080	SAEC	small airway:	n/a
10	chr4:79096535-79096585	NT2-D1	testis:	n/a
11	chr4:79106308-79106358	HRPEpiC	eye:	n/a
12	chr4:79101988-79102038	ProgFib	skin:	n/a
13	chr4:79106308-79106358	GM12891	blood:	n/a
14	chr4:79102901-79102951	NHBE	bronchial:	n/a
15	chr4:79102707-79102757	K562	blood:	n/a
16	chr4:79102910-79102960	AoSMC	blood vessel:	n/a
17	chr4:79106308-79106358	U87	brain:	n/a
18	chr4:79101988-79102038	GM12891	blood:	n/a
19	chr4:79103244-79103294	NT2-D1	testis:	n/a
20	chr4:79103290-79103340	AG04450	lung:	fetal
21	chr4:79103126-79103176	NH-A	brain:	n/a
22	chr4:79091679-79091729	PANC-1	pancreas:	n/a
23	chr4:79103244-79103294	LNCaP	prostate:	n/a
24	chr4:79103030-79103080	IMR90	lung:	fetal
25	chr4:79096535-79096585	SAEC	small airway:	n/a
26	chr4:79102901-79102951	NH-A	brain:	n/a
27	chr4:79102910-79102960	NHDF-neo	bronchial:	n/a
28	chr4:79103030-79103080	HRE	kidney:	n/a
29	chr4:79106308-79106358	HEEpiC	esophagus:	n/a
30	chr4:79103290-79103340	BJ	skin:	n/a
31	chr4:79096535-79096585	NH-A	brain:	n/a
32	chr4:79093019-79093069	A549	lung:	n/a
33	chr4:79102707-79102757	LNCaP	prostate:	n/a
34	chr4:79103030-79103080	CMK	blood:	n/a
35	chr4:79083545-79083595	NHDF-neo	bronchial:	n/a
36	chr4:79096535-79096585	HIPEpiC	eye:	n/a
37	chr4:79102910-79102960	HCM	heart:	n/a
38	chr4:79102910-79102960	HepG2	liver:	n/a
39	chr4:79096535-79096585	LNCaP	prostate:	n/a
40	chr4:79103030-79103080	NHBE	bronchial:	n/a
41	chr4:79083545-79083595	HepG2	liver:	n/a
42	chr4:79103030-79103080	T-47D	breast:	n/a
43	chr4:79096535-79096585	MCF-7	breast:	n/a
44	chr4:79101988-79102038	Hepatocyte	liver:	n/a
45	chr4:79083545-79083595	Hepatocyte	liver:	n/a
46	chr4:79106308-79106358	Jurkat	blood:	n/a
47	chr4:79101988-79102038	PANC-1	pancreas:	n/a
48	chr4:79102901-79102951	LNCaP	prostate:	n/a
49	chr4:79102901-79102951	AoSMC	blood vessel:	n/a
50	chr4:79103244-79103294	NHBE	bronchial:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:79097455..79099663-chr4:79105000..79107358,2	MCF-7	breast:
2	chr4:78980297..78981139-chr4:79092342..79093264,2	MCF-7	breast:
3	chr4:79093805..79095382-chr4:79119242..79121206,2	K562	blood:
4	chr4:79085535..79087352-chr4:79088663..79090965,2	K562	blood:
5	chr4:79091323..79093499-chr4:79096107..79097895,2	MCF-7	breast:
6	chr4:79085535..79087352-chr4:79088663..79090965,2	K562	blood:
7	chr4:79097455..79099663-chr4:79105000..79107358,2	MCF-7	breast:
8	chr4:79091323..79093499-chr4:79096107..79097895,2	MCF-7	breast:
9	chr4:79080375..79082514-chr4:79085692..79087997,2	MCF-7	breast:
10	chr4:79082865..79083529-chr6:109330266..109331128,2	Hela-S3	cervix:
11	chr4:79104998..79106622-chr4:79109198..79111577,2	K562	blood:
12	chr4:79080375..79082514-chr4:79085692..79087997,2	MCF-7	breast:

No data

Variant related genes	Relation type
SERBP1P5	TF binding region
ENSG00000221183	TF binding region
SERBP1P5	CpG island
ENSG00000221183	CpG island
ENSG00000080546	chromatin interactions
ENSG00000221183	chromatin interactions

Extended variants
information (count: 1001 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1001 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200489858	chr4:79082330-79082331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190627479	chr4:79082334-79082335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183180581	chr4:79082516-79082517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535269288	chr4:79082523-79082524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558400618	chr4:79082554-79082555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374698884	chr4:79082595-79082596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187838126	chr4:79082620-79082621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543472588	chr4:79082639-79082640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371731255	chr4:79082647-79082648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574082397	chr4:79082656-79082657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571842941	chr4:79082658-79082659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561821136	chr4:79082741-79082742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116624190	chr4:79082746-79082747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7698326	chr4:79082750-79082751	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs564395038	chr4:79082793-79082794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532920044	chr4:79082794-79082795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557333777	chr4:79082814-79082815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192426731	chr4:79082864-79082865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569722791	chr4:79082888-79082889	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570727357	chr4:79082896-79082897	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113326479	chr4:79082922-79082923	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs71214399	chr4:79082926-79082927	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144099400	chr4:79082927-79082928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368387613	chr4:79082932-79082933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371846907	chr4:79082937-79082938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535243585	chr4:79082941-79082942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375291872	chr4:79082942-79082943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs184108505	chr4:79082966-79082967	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs62308026	chr4:79082974-79082975	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs74702306	chr4:79083024-79083025	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs187459173	chr4:79083057-79083058	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs557999316	chr4:79083068-79083069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147962363	chr4:79083082-79083083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs35937599	chr4:79083091-79083092	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs17420328	chr4:79083162-79083163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs542257625	chr4:79083194-79083195	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573984239	chr4:79083213-79083214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141714260	chr4:79083241-79083242	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs17327	chr4:79083381-79083382	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184735652	chr4:79083402-79083403	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566746960	chr4:79083415-79083416	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564358241	chr4:79083423-79083424	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572833383	chr4:79083427-79083428	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113904342	chr4:79083455-79083456	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544667613	chr4:79083473-79083474	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564759582	chr4:79083479-79083480	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs147096609	chr4:79083480-79083481	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528891230	chr4:79083489-79083490	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs10518194	chr4:79083490-79083491	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs78316934	chr4:79083531-79083532	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79071000-79083600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:79071200-79082600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr4:79071400-79096600	Weak transcription	Pancreas	Pancrea
4	chr4:79078000-79082400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr4:79078000-79083800	Weak transcription	Fetal Intestine Large	intestine
6	chr4:79078200-79082400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr4:79078200-79083600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:79078200-79085000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:79078200-79094200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:79078400-79083000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr4:79078400-79083400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:79078400-79083600	Weak transcription	HepG2	liver
13	chr4:79078400-79095600	Weak transcription	Psoas Muscle	Psoas
14	chr4:79081600-79083400	Weak transcription	Fetal Kidney	kidney
15	chr4:79081600-79084400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr4:79081800-79084200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:79082000-79084000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:79082400-79083400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:79082400-79083400	Weak transcription	Fetal Intestine Small	intestine
20	chr4:79082400-79085200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr4:79082400-79086600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr4:79082600-79084200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:79083000-79084200	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:79083000-79084400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:79083200-79083400	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr4:79083200-79083800	Enhancers	Fetal Heart	heart
27	chr4:79083400-79083600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr4:79083400-79084000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:79083400-79084000	Enhancers	Fetal Intestine Small	intestine
30	chr4:79083400-79084200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:79083400-79084200	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr4:79083400-79084200	Enhancers	Fetal Kidney	kidney
33	chr4:79083400-79085000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:79083600-79084000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr4:79083600-79084200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr4:79083600-79084200	Enhancers	H9 Cell Line	embryonic stem cell
37	chr4:79083600-79084200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr4:79083600-79084200	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr4:79083600-79086200	Enhancers	HepG2	liver
40	chr4:79083800-79084200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:79083800-79084200	Enhancers	Fetal Intestine Large	intestine
42	chr4:79083800-79084200	Enhancers	HMEC	breast
43	chr4:79083800-79084200	Enhancers	NHEK	skin
44	chr4:79083800-79093000	Weak transcription	Fetal Heart	heart
45	chr4:79084000-79085000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:79084000-79085200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:79084000-79086600	Weak transcription	Fetal Intestine Small	intestine
48	chr4:79084200-79085200	Weak transcription	Fetal Kidney	kidney
49	chr4:79084200-79086200	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr4:79084200-79086400	Weak transcription	Fetal Intestine Large	intestine

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